It is not appropriate to gauge the probability of a side effect happening based on the quantity of suspected reactions recorded in the FDA Adverse Event Reporting System. Not every adverse event or medication error involving a product is reported to the FDA. Numerous factors, like the length of...
(mOS) for patients with primary refractory AML; mOS was 31.2 months for the uproleselan arm compared to 10.1 months for the placebo arm in this subgroup Adverse events for uproleselan were consistent with known side effect profiles of chemotherapy used in the study Advancing discussions with ...
Because there is no specific ICD code for amlodipine overdose or toxicity, patients were identified via ICD codes for primary or secondary diagnosis of CCB poisoning (ICD-10 T46.1X1A, T46.1X1B), poisoning by other antihypertensive agents (ICD-9 972.6 and CCB adverse reaction (ICD-10 T46.1X5...
Because there is no specific ICD code for amlodipine overdose or toxicity, patients were identified via ICD codes for primary or secondary diagnosis of CCB poisoning (ICD-10 T46.1X1A, T46.1X1B), poisoning by other antihypertensive agents (ICD-9 972.6 and CCB adverse reaction (ICD-10 T46.1X5...